About this trial
Breastfeeding provides well-established and "irreplaceable" health benefits for both mothers and infants. However, breastfeeding rates in France remain among the lowest in Europe and are strongly associated with socioeconomic status. Mothers experiencing severe socioeconomic deprivation, including those facing housing instability or migration-related challenges, may encounter additional barriers to breastfeeding, such as social isolation, limited access to health information, and linguistic or cultural obstacles.
Peer and community support have been shown to positively influence breastfeeding initiation and continuation. The Relais Allaitement Program (PRALL) is a peer-support program designed to promote breastfeeding and support early parenting through trained volunteer mothers. The PARTAGE project aims to adapt and pilot the PRALL program for mothers experiencing severe socioeconomic deprivation receiving care at the maternity unit of the Hôpital Femme Mère Enfant (HFME), in Bron, France.
This prospective, interventional, non-comparative feasibility study will evaluate the acceptability and feasibility of a peer-support breastfeeding program delivered by trained experienced mothers (peer supporters).
The intervention includes:
* the adaptation of PRALL educational materials and training to the needs of vulnerable populations using participatory approaches and accessible communication principles, * the recruitment and training of two nursery nurses from the maternity unit to become network coordinators of the peer-support network, * the recruitment of experienced mothers who will be trained by the 2 network coordinators, to become breastfeeding peer supporters, * and the implementation of breastfeeding support by peer supporters for eligible mothers.
Eligible mothers experiencing severe socioeconomic deprivation will be offered support from a trained peer supporter during the postpartum period.
The primary outcome is the number of completed support interventions, defined as to have at least two in-person mother/peer supporter contacts and to last at least one month, unless breastfeeding cessation or infant death occurs earlier. Qualitative interviews with participating mothers and peer supporters will also be conducted to explore barriers and facilitators to breastfeeding support in this population.
The results will inform the adaptation of the PRALL program for vulnerable populations and assess the feasibility of implementing a peer-support breastfeeding intervention in this context. Findings may guide the development of a larger multicenter study to evaluate the impact of peer-support programs on breastfeeding outcomes among socially disadvantaged populations in France and potentially across Europe.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Mother with at least one infant hospitalized in the maternity or neonatal unit at the Hôpital Femme Mère Enfant (HFME)
Who Intents to breastfeed
Who is in a severe socioeconomic deprivation
Having sufficient proficiency in French or in one of the languages spoken by the available peer supporters to allow communication
Disqualifiers
- Having a medical contraindication to breastfeeding
Having an infant with a known congenital condition with life-threatening prognosis
Having a severe psychiatric condition considered incompatible with participation in the peer-support intervention
Being under legal guardianship
Trial population
The study population consists of mothers experiencing severe socioeconomic deprivation with an infant hospitalized in the maternity or neonatal unit at the Hôpital Femme Mère Enfant (HFME), France. Eligible participants are adult mothers (≥18 years) who intend to breastfeed, have sufficient proficiency in French or a language spoken by available peer supporters, and provide oral agreement to participate. Mothers will be identified and recruited during their hospital stay. Approximately 20 eligible mothers are seen monthly in the unit. Based on eligibility criteria, expected refusal rates, and peer supporter availability (maximum two concurrent supports per peer), an estimated 5 to 8 mothers will be enrolled per month over 6 months, for a total sample of approximately 30 to 50 participants. Exclusion criteria include medical contraindications to breastfeeding, infants with life-threatening conditions, severe psychiatric conditions incompatible with participation, and legal guardianship.
Trial design
Cohort
Prospective
Treatments tested in this trial
Peer-Support Breastfeeding Intervention
BehavioralThe intervention consists of a peer-to-peer breastfeeding support, delivered over a 2-month period, designed to ensure continuity of support after discharge from the maternity ward, particularly for mothers in highly socioeconomic deprivation who are at high risk of losing access to care. An initial face-to-face meeting with a trained peer supporter is offered during the hospital stay. Another peer supporter may be reassigned if necessary, in accordance with the network coordinators. The intervention includes weekly contacts during the first month and biweekly contacts during the second month (approximately 6 contacts total), unless breastfeeding cessation or infant death occurs earlier. Contacts are preferably conducted face-to-face at a location chosen by the mother; telephone or video contacts may be used when needed, with at least 2 in-person meetings expected. The intervention is flexible and tailored to individual needs to support breastfeeding and maternal well-being.
Treatment groups
Trial outcomes
Primary outcomes
Number of completed peer-support breastfeeding interventions defined by at least two in-person mother/peer supporter contacts and a duration and to last at least one month (unless breastfeeding cessation or infant death occurs earlier)
Acceptability will be assessed through the number of completed peer-support interventions and monitoring of peer supporter activity. Data regarding contacts (type of contact, topic discussed, and duration) will be reported by the peer mentors via phone/SMS to the coordination center and monthly meetings with network coordinators. Implementation data will be collected and analyzed descriptively by the coordination team to assess feasibility, fidelity, and maintenance of the adapted program. Confidentiality will be ensured.
Sponsors and contacts
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